Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S5H730
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0034453 | microtubule anchoring | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 11 |
GO:0008047 | enzyme activator activity | 3 | 11 |
GO:0030234 | enzyme regulator activity | 2 | 11 |
GO:0030695 | GTPase regulator activity | 4 | 11 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 11 |
GO:0098772 | molecular function regulator activity | 1 | 11 |
GO:0140677 | molecular function activator activity | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 214 | 218 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.715 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.758 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.405 |
DEG_SCF_FBW7_2 | 322 | 328 | PF00400 | 0.561 |
DEG_SPOP_SBC_1 | 439 | 443 | PF00917 | 0.886 |
DEG_SPOP_SBC_1 | 444 | 448 | PF00917 | 0.905 |
DOC_CDC14_PxL_1 | 474 | 482 | PF14671 | 0.721 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.559 |
DOC_CYCLIN_RxL_1 | 47 | 57 | PF00134 | 0.661 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.698 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.637 |
DOC_MAPK_gen_1 | 241 | 250 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 256 | 265 | PF00069 | 0.356 |
DOC_MAPK_HePTP_8 | 238 | 250 | PF00069 | 0.403 |
DOC_MAPK_HePTP_8 | 255 | 267 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 48 | 55 | PF00149 | 0.671 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.425 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.823 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.871 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.839 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.823 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.709 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.838 |
LIG_14-3-3_CanoR_1 | 341 | 346 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 65 | 74 | PF00244 | 0.676 |
LIG_Actin_WH2_2 | 22 | 38 | PF00022 | 0.655 |
LIG_Actin_WH2_2 | 89 | 104 | PF00022 | 0.711 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.729 |
LIG_BIR_III_4 | 146 | 150 | PF00653 | 0.733 |
LIG_CAP-Gly_1 | 520 | 528 | PF01302 | 0.719 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.522 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.409 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.425 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.395 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.822 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.702 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.593 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.544 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.669 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.831 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.390 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.700 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 501 | 510 | PF02991 | 0.751 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.573 |
LIG_MYND_1 | 478 | 482 | PF01753 | 0.727 |
LIG_PDZ_Class_3 | 523 | 528 | PF00595 | 0.712 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.474 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.615 |
LIG_PTB_Apo_2 | 497 | 504 | PF02174 | 0.834 |
LIG_PTB_Phospho_1 | 497 | 503 | PF10480 | 0.835 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.549 |
LIG_SH3_1 | 345 | 351 | PF00018 | 0.499 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.558 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.486 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.393 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.779 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.711 |
LIG_SUMO_SIM_anti_2 | 69 | 76 | PF11976 | 0.611 |
LIG_SUMO_SIM_par_1 | 209 | 215 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 56 | 62 | PF11976 | 0.715 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.903 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.732 |
LIG_TYR_ITIM | 78 | 83 | PF00017 | 0.627 |
LIG_WRC_WIRS_1 | 503 | 508 | PF05994 | 0.743 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.742 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.607 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.671 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.849 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.855 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.648 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.860 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.723 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.636 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.829 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.898 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.641 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.525 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.792 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.533 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.526 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.674 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.640 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.497 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.775 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.836 |
MOD_GlcNHglycan | 44 | 48 | PF01048 | 0.773 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.847 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.806 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.531 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.662 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.530 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.482 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.676 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.837 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.803 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.623 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.449 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.652 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.663 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.569 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.389 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.669 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.543 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.449 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.663 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.805 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.617 |
MOD_Plk_2-3 | 217 | 223 | PF00069 | 0.389 |
MOD_Plk_2-3 | 426 | 432 | PF00069 | 0.861 |
MOD_Plk_2-3 | 502 | 508 | PF00069 | 0.839 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.518 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.744 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.385 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.401 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.581 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.586 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.560 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.843 |
MOD_SUMO_rev_2 | 299 | 306 | PF00179 | 0.436 |
TRG_DiLeu_BaEn_1 | 130 | 135 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_2 | 234 | 240 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.727 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.744 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.611 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.389 |
TRG_NLS_MonoExtN_4 | 183 | 189 | PF00514 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Z4 | Leptomonas seymouri | 60% | 100% |
A0A0S4J201 | Bodo saltans | 49% | 100% |
A0A1X0P6T6 | Trypanosomatidae | 53% | 100% |
A0A3R7NEX5 | Trypanosoma rangeli | 52% | 100% |
A4H9G1 | Leishmania braziliensis | 79% | 99% |
A4HXS8 | Leishmania infantum | 98% | 99% |
D0A060 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9ARJ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
V5BRP2 | Trypanosoma cruzi | 52% | 100% |